510(k) K263208 ยท HRX Arthroscope
Vantage Lumbar Decompression Kit
| Applicant | SurGenTec, LLC, Boca Raton FL, US |
| Decision | Substantially Equivalent, Oct 14, 2026 |
| Received | Sep 14, 2026 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K263208
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.